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GB437566A - Manufacture of textile assistants - Google Patents

Manufacture of textile assistants

Info

Publication number
GB437566A
GB437566A GB4924/35A GB492435A GB437566A GB 437566 A GB437566 A GB 437566A GB 4924/35 A GB4924/35 A GB 4924/35A GB 492435 A GB492435 A GB 492435A GB 437566 A GB437566 A GB 437566A
Authority
GB
United Kingdom
Prior art keywords
radicle
product
cetyl
piperidine
lauryl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB4924/35A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF Schweiz AG
Original Assignee
Gesellschaft fuer Chemische Industrie in Basel CIBA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Gesellschaft fuer Chemische Industrie in Basel CIBA filed Critical Gesellschaft fuer Chemische Industrie in Basel CIBA
Publication of GB437566A publication Critical patent/GB437566A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/02Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements
    • C07D295/027Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements containing only one hetero ring
    • C07D295/03Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements containing only one hetero ring with the ring nitrogen atoms directly attached to acyclic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C291/00Compounds containing carbon and nitrogen and having functional groups not covered by groups C07C201/00 - C07C281/00
    • C07C291/02Compounds containing carbon and nitrogen and having functional groups not covered by groups C07C201/00 - C07C281/00 containing nitrogen-oxide bonds
    • C07C291/04Compounds containing carbon and nitrogen and having functional groups not covered by groups C07C201/00 - C07C281/00 containing nitrogen-oxide bonds containing amino-oxide bonds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/02Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/75Amino oxides

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

Tertiary amines containing an aliphatic or hydroaromatic radicle of at least six carbon atoms are treated with an oxidizing-agent capable of converting a tertiary amine into its oxide. The amines treated may be of the type NRR<1>R<11>, where R is capryl, lauryl, stearyl, cetyl, octadecenyl or like radicle and R<1> and R<11> are the same or different lower alkyl groups such as methyl or ethyl; alternatively, R<1>, R<11> and the nitrogen atom may form a heterocyclic ring, such as a piperidine or pyrollidine ring. The radicle R is not necessarily linked directly to the nitrogen atom, but may be linked through an aromatic nucleus or a group such as --OCH2CH2-- or --C(O)-NHCH2CH2--. Specified oxidizing agents are Caro's acid, hydrogen peroxide and ozone. The reaction may be effected in the cold in water or an organic solvent such as acetone or chloroform. The products are useful as textile assistants, particularly as wetting, washing, levelling, emulsifying and softening agents, and agents for rendering direct dyeings fast to water. Examples are given of the preparation of oxides from (1) 4-dimethylamino-1-laurophenone, prepared from dimethylaniline and lauric acid chloride in the presence of zinc chloride, (2) a ketone obtained from dimethylaniline and stearic acid chloride, (3) 1-dodecyl-4-dimethylaminobenzene, prepared by reducing the ketone used in example 1, (4) lauryldimethylamine, (5) cetyldimethylamine, (6) stearoyldiethylethylenediamine, (7) cetyldiethylamine, (8) lauryldiethylamine, (9) N-lauryl- or N-cetyl-piperidine and (10) the reaction product of chlorinated paraffin wax and dimethylamine. In examples of the use of the products, (a) wool in the yolk is washed in a bath containing sodium carbonate and the product of example 1; (b) woollen rags soiled with mineral oil are washed in a bath containing the product of example 1; (c) cotton is dyed with Cibanone blue 3G in a bath containing sodium hydrosulphite, sodium hydroxide and the product of example 1; (d) wool is dyed with the chromium compound of the dye 5-nitro-2-aminophenol --> 2-aminonaphthalene-6-sulphonic acid in a bath containing sulphuric acid and the product of example 4; (e) wool yarn is wetted with an aqueous solution of the product of example 4.ALSO:As emulsifying agents in the textile industry, use is made of the oxides of tertiary amines containing an aliphatic or hydroaromatic radicle of at least six carbon atoms. The amines from which the oxides are derived may be of the type NRR<1>R<11>, where R is capryl, lauryl, stearyl, cetyl, octadecenyl or like radicle and R<1> and R<11> are the same or different lower alkyl groups such as methyl or ethyl; alterantively, R<1>, R<11> and the nitrogen atom may form a heterocyclic ring, such as a piperidine or pyrollidine ring. The radicle R is not necessarily linked directly to the nitrogen atom, but may be linked through an aromatic nucleus or a group such as -OCH2CH2- or -C(O)NHCH2CH2-. Examples are given of the preparation of oxides from (1) 4-dimethylamino-1-laurophenone, (2) a ketone obtained from dimethylaniline and stearic acid chloride, (3) 1-dodecyl-4-dimethylaminobenzene, (4) lauryldimethylamine, (5) p cetyldimethylamine, (6) stearoyldiethylethylenediamine, (7) cetyldiethylamine, (8) lauryldiethylamine, (9) N-lauryl- or N-cetyl-piperidine and (10) the reaction product of chlorinated paraffin wax and dimethylamine.
GB4924/35A 1934-02-16 1935-02-15 Manufacture of textile assistants Expired GB437566A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH437566X 1934-02-16

Publications (1)

Publication Number Publication Date
GB437566A true GB437566A (en) 1935-10-31

Family

ID=4515102

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4924/35A Expired GB437566A (en) 1934-02-16 1935-02-15 Manufacture of textile assistants

Country Status (4)

Country Link
ES (1) ES137248A1 (en)
FR (1) FR786911A (en)
GB (1) GB437566A (en)
NL (1) NL40691C (en)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2999068A (en) * 1959-04-27 1961-09-05 Procter & Gamble Personal use detergent lotion
US3001945A (en) * 1959-04-29 1961-09-26 Procter & Gamble Liquid detergent composition
US3085982A (en) * 1959-04-22 1963-04-16 Procter & Gamble Liquid detergent composition
US3086943A (en) * 1959-06-10 1963-04-23 Procter & Gamble Shampoo containing amine oxide
US3098794A (en) * 1959-08-08 1963-07-23 Therachemie Chem Therapeut Process for treating human hair with amino oxide compositions
US3223647A (en) * 1959-04-20 1965-12-14 Procter & Gamble Mild detergent compositions
US3317430A (en) * 1960-05-05 1967-05-02 Lever Brothers Ltd Detergent compositions
US3332999A (en) * 1963-12-10 1967-07-25 Ethyl Corp Process for preparation of amine oxides
US3336387A (en) * 1964-02-28 1967-08-15 Shell Oil Co Tertiary amine oxides
US3336388A (en) * 1964-01-20 1967-08-15 Archer Daniels Midland Co Preparation of anhydrous amine oxides
US6323170B1 (en) 1994-10-28 2001-11-27 The Procter & Gamble Co. Floor cleaners which provide improved burnish response

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1219614B (en) * 1960-07-14 1966-06-23 Henkel & Cie Gmbh laundry detergent

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3223647A (en) * 1959-04-20 1965-12-14 Procter & Gamble Mild detergent compositions
US3085982A (en) * 1959-04-22 1963-04-16 Procter & Gamble Liquid detergent composition
US2999068A (en) * 1959-04-27 1961-09-05 Procter & Gamble Personal use detergent lotion
US3001945A (en) * 1959-04-29 1961-09-26 Procter & Gamble Liquid detergent composition
US3086943A (en) * 1959-06-10 1963-04-23 Procter & Gamble Shampoo containing amine oxide
US3098794A (en) * 1959-08-08 1963-07-23 Therachemie Chem Therapeut Process for treating human hair with amino oxide compositions
US3317430A (en) * 1960-05-05 1967-05-02 Lever Brothers Ltd Detergent compositions
US3332999A (en) * 1963-12-10 1967-07-25 Ethyl Corp Process for preparation of amine oxides
US3336388A (en) * 1964-01-20 1967-08-15 Archer Daniels Midland Co Preparation of anhydrous amine oxides
US3336387A (en) * 1964-02-28 1967-08-15 Shell Oil Co Tertiary amine oxides
US6323170B1 (en) 1994-10-28 2001-11-27 The Procter & Gamble Co. Floor cleaners which provide improved burnish response

Also Published As

Publication number Publication date
NL40691C (en)
FR786911A (en) 1935-09-14
ES137248A1 (en) 1935-07-16

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